Total variants with conflicting interpretations: 8
HGVS | dbSNP | gnomAD frequency |
---|---|---|
NM_000243. |
rs104895094 | 0.00506 |
NM_000350. |
rs1800552 | 0.00153 |
NM_000104. |
rs79204362 | 0.00125 |
NM_000488. |
rs121909551 | 0.00092 |
NM_000261. |
rs74315339 | 0.00001 |
NM_000546. |
rs28934574 | 0.00001 |
NM_201253. |
rs398124615 | |
Single allele |